Theoretical and Natural Science

- The Open Access Proceedings Series for Conferences


Theoretical and Natural Science

Vol. 24, 20 December 2023


Open Access | Article

The use of oncolytic virus to combat neuroblastoma

Victor Zhao * 1 , Linxiaoshi Hu 2 , Yishan Li 3 , Elisa Pan 4
1 St. George’s Senior School
2 Chinese University of Hong Kong
3 Wellington College International Shanghai
4 St. Stephen’s School

* Author to whom correspondence should be addressed.

Theoretical and Natural Science, Vol. 24, 52-58
Published 20 December 2023. © 2023 The Author(s). Published by EWA Publishing
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Citation Victor Zhao, Linxiaoshi Hu, Yishan Li, Elisa Pan. The use of oncolytic virus to combat neuroblastoma. TNS (2023) Vol. 24: 52-58. DOI: 10.54254/2753-8818/24/20231094.

Abstract

Neuroblastoma is a type of cancer that arises from immature nerve cells in the body and often appears in children. The current treatment of chemotherapy and radiotherapy is not a successful method of treatment due to its harm to the child’s body and its inability to effectively pass the blood-brain barrier (BBB) in the brain to effectively target the tumor. Recent studies into the field of oncolytic viruses have shown the possibility to target neuroblastoma cancer cells in the brain by engineering specific viruses to express NY-ESO-1, an antigen that is tumor-specific and commonly expressed in neuroblastoma. Research also showed a method to integrate protein A into the envelope protein of retroviruses which allows monoclonal antibodies’ Fc region to bind with the virus, allowing specificity to an antigen. This paper combines the ideas of previous studies to design a novel model of oncolytic virus treatment that specifically targets neuroblastoma. Since the oncolytic virus can be injected directly at the site and the virus is small enough to penetrate the BBB, the paper hypothesize that the model is a valid treatment for neuroblastoma in children.

Keywords

NY-ESO-1, HSV-1, Protein-A Integration, Monoclonal Antibodies, GM-CSF

References

1. Colon. (2011) Neuroblastoma. Advances in pediatrics. 58(1):297-311

2. Mohammad et al. (2008) A review of neuroblastoma: prevalence, diagnosis, related genetic factors, and treatment. Iran J Ped Hematol Oncol. Vol 8. No 4, 237-246

3. Sung KW. (2012) Treatment of high-risk neuroblastoma. Korean Journal of Pediatrics. 55(4):115-20.

4. Michael et al. (2018) Isolation and characterization of NY-ESO-1–specific T cell receptors restricted on various MHC molecules. Proc Natl Acad Sci USA. 115(45): E10702-E10711

5. BL Liu et al. (2003) ICP34.5 deleted herpes simplex virus with enhanced oncolytic, immune-stimulating, and anti-tumor properties. Gene Ther. 10(4):292-303

6. KOUKI et al. (2001) Antibody-Directed Targeting of Retroviral Vectors via Cell. J Virol. 75(17):8016-20.

7. Johnson LA, et al. (2006) Gene transfer of tumor-reactive TCR confers both high avidity and tumor reactivity to nonreactive peripheral blood mononuclear cells and tumor-infiltrating lymphocytes. J Immunol. 177:6548–6559.

8. Hansford et al. (2004) Mechanisms of embryonal tumor initiation: distinct roles for MYCN expression and MYCN amplification. Proc Natl Acad Sci USA. 101: 12664– 12669.

9. Althoff et al. (2015) A Cre-conditional MYCN-driven neuroblastoma mouse. Oncogene. 34: 3357–3368

10. Chan et al. (1997) MYCN protein expression as a predictor of neuroblastoma prognosis. Clin Cancer Res. 3(10):1699-706.

Data Availability

The datasets used and/or analyzed during the current study will be available from the authors upon reasonable request.

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Volume Title
Proceedings of the 3rd International Conference on Biological Engineering and Medical Science
ISBN (Print)
978-1-83558-221-3
ISBN (Online)
978-1-83558-222-0
Published Date
20 December 2023
Series
Theoretical and Natural Science
ISSN (Print)
2753-8818
ISSN (Online)
2753-8826
DOI
10.54254/2753-8818/24/20231094
Copyright
20 December 2023
Open Access
This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited

Copyright © 2023 EWA Publishing. Unless Otherwise Stated